Coalescence in an interface-modified polymer blend as studied by light scattering measurements
The influence of A—B diblock copolymers on coalescence in A:B blends has been studied by rheo-optical measurements and electron microscopy. Divergent criteria and experimental evidence appear in the literature on the block copolymer (BC) molecular weight ( M W) and volume fraction ( ϕ bc) when the r...
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Published in | Polymer (Guilford) Vol. 37; no. 3; pp. 509 - 517 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Oxford
Elsevier Ltd
01.02.1996
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | The influence of A—B diblock copolymers on coalescence in A:B blends has been studied by rheo-optical measurements and electron microscopy. Divergent criteria and experimental evidence appear in the literature on the block copolymer (BC) molecular weight (
M
W) and volume fraction (
ϕ
bc) when the requirement is the BC to reside at the interface. In the present study the block chain lengths were chosen shorter than the corresponding homopolymers as a starting point. For selected model systems it was found that symmetrical diblock copolymers with
ϕ
bc ≥ 1% were most effective for inhibiting coalescence. However, rheo-optical measurements revealed that the stabilization effect is not unconditional during the flow; coalescence is prevented for a time which decreases with increasing shear rate due to removal of the BC away from the interface. The origin of the observed behaviour is discussed based on various mechanisms: shear-induced mutual compatibility between components, squeeze-out/drainage of the interfacial layer, frictional pull-out of BC chains, collision-induced entrapment of BC between interfaces, encapsulation of the BC based on the concept of elastic interfacial curvature. |
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ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/0032-3861(96)82923-5 |